Canonical Allele Identifier: PA180755
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 177778
ClinVar RCV Id: RCV000158978 RCV000212761 RCV000431995 RCV000433097 RCV000421993 RCV000427184 RCV000439216 RCV000445150 RCV000442594 RCV000421327 RCV000430288 RCV001066799 RCV003998247 RCV001813397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gly12Ser
CA180753
NM_002524.5:c.34G>A